Package 11788-037-60

Brand: metformin hydrochloride

Generic: metformin hydrochloride extended-release tablets
NDC Package

Package Facts

Identity

Package NDC 11788-037-60
Digits Only 1178803760
Product NDC 11788-037
Description

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (11788-037-60)

Marketing

Marketing Status
Marketed Since 2025-12-15
Brand metformin hydrochloride
Generic metformin hydrochloride extended-release tablets
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5ad15c75-5a99-4fa0-96f8-21e75064eff3", "openfda": {"unii": ["786Z46389E"], "rxcui": ["1807894", "1807917"], "spl_set_id": ["96c8a89d-99db-24b1-e053-2a95a90ac2b8"], "manufacturer_name": ["AiPing Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (11788-037-60)", "package_ndc": "11788-037-60", "marketing_start_date": "20251215"}], "brand_name": "Metformin Hydrochloride", "product_id": "11788-037_5ad15c75-5a99-4fa0-96f8-21e75064eff3", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "11788-037", "generic_name": "Metformin Hydrochloride Extended-Release Tablets", "labeler_name": "AiPing Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA209993", "marketing_category": "ANDA", "marketing_start_date": "20251215", "listing_expiration_date": "20271231"}